Evidence map›Paper›PMID 28823027›Full record

Trial reportInternational journal of clinical oncology2018

A prospective study of palonosetron for prevention of chemotherapy-induced nausea and vomiting in malignant lymphoma patients following highly emetogenic chemotherapy.

Tsutomu Takahashi, Takahiro Okada, Fumiyoshi Ikejiri, Shunsuke Ito, Yusuke Okada, Fumimasa Takahashi, Satoshi Kumanomido, Yumi Jo, Koji Adachi, Chie Onishi and 5 more

Abstract readClinical Trial, Phase II
PubMed Publisher
In one paragraph

Trial report in International journal of clinical oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 83% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 3 institutions in 1 country.

Tsutomu TakahashiDepartment of Oncology/Hematology, Shimane University Hospital, 89-1 Enya-cho, Izumo-shi, Shimane, 693-8501, Japan. ben2106t@med.shimane-u.ac.jp.
Takahiro OkadaDepartment of Oncology/Hematology, Shimane University Hospital, 89-1 Enya-cho, Izumo-shi, Shimane, 693-8501, Japan.
Fumiyoshi IkejiriDepartment of Oncology/Hematology, Shimane University Hospital, 89-1 Enya-cho, Izumo-shi, Shimane, 693-8501, Japan.
Shunsuke ItoDepartment of Oncology/Hematology, Shimane University Hospital, 89-1 Enya-cho, Izumo-shi, Shimane, 693-8501, Japan.
Yusuke OkadaDepartment of Oncology/Hematology, Shimane University Hospital, 89-1 Enya-cho, Izumo-shi, Shimane, 693-8501, Japan.
Fumimasa TakahashiDepartment of Oncology/Hematology, Shimane University Hospital, 89-1 Enya-cho, Izumo-shi, Shimane, 693-8501, Japan.
Satoshi KumanomidoDepartment of Oncology/Hematology, Shimane University Hospital, 89-1 Enya-cho, Izumo-shi, Shimane, 693-8501, Japan.
Yumi JoDepartment of Oncology/Hematology, Shimane University Hospital, 89-1 Enya-cho, Izumo-shi, Shimane, 693-8501, Japan.
Koji AdachiDepartment of Hematology and Oncology, National Hospital Organization, Yonago Medical Center, Yonago, Japan.
Chie OnishiDepartment of Oncology/Hematology, Shimane University Hospital, 89-1 Enya-cho, Izumo-shi, Shimane, 693-8501, Japan.
Koshi KawakamiDepartment of Clinical Oncology, Shimane Prefectural Central Hospital, Izumo, Japan.
Takaaki MiyakeDepartment of Oncology/Hematology, Shimane University Hospital, 89-1 Enya-cho, Izumo-shi, Shimane, 693-8501, Japan.
Masaya InoueDepartment of Oncology/Hematology, Shimane University Hospital, 89-1 Enya-cho, Izumo-shi, Shimane, 693-8501, Japan.
Ritsuro SuzukiDepartment of Oncology/Hematology, Shimane University Hospital, 89-1 Enya-cho, Izumo-shi, Shimane, 693-8501, Japan.
Junji SuzumiyaDepartment of Oncology/Hematology, Shimane University Hospital, 89-1 Enya-cho, Izumo-shi, Shimane, 693-8501, Japan.
Shimane University Hospital · JPNational Hospital Organization · JPShimane Prefectural Central Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChemotherapy-induced nausea and vomiting (CINV) is a troublesome issue in chemotherapy for cancer patients. A second-generation 5HT

methodsChemotherapy-naïve lymphoma patients who were treated with highly emetogenic chemotherapy (HEC) received a single intravenous bolus of palonosetron, 0.75 mg/body, before chemotherapy on day 1 during the first course of chemotherapy. The occurrence of CINV was assessed using the Multinational Association for Supportive Care in Cancer (MASCC) antiemesis tool, which was recorded by patients during the first course of chemotherapy.

resultsA total of 59 patients were enrolled, and 49 patients were eligible and evaluated. The complete response (CR) rate was 93.9% (95% confidence interval 83.1-98.7%) at 0-120 h post-chemotherapy. The proportion of patients who developed nausea of any grade and vomiting at 0-120 h post-chemotherapy was 34.7 and 6.1%, respectively. Although treatment-related adverse events were observed in 36 (73.5%) patients, these were mild and they recovered by the next cycle of chemotherapy.

conclusionThe present study demonstrated that a single dose of palonosetron was highly effective and safe for the prevention of CINV in lymphoma patients.

Indexed as

Administration, IntravenousAdultAgedAged, 80 and overAntiemeticsAntineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsFemaleHumansIsoquinolinesLymphomaMaleMiddle AgedNauseaPalonosetronProspective StudiesAntiemeticsIsoquinolinesPalonosetronQuinuclidinesChemotherapyLymphomaNauseaPalonosetronVomiting

Identifiers

PMID28823027
OpenAlexW2748432207

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.